Similar articles for PMID: 6782878

Year	Number of Results
1965	2
1971	1
1977	1
1979	4
1980	3
1981	1
1982	5
1983	4
1984	4
1986	1
1990	1
1993	5
1994	2
1996	3
1998	3
1999	2
2001	2
2003	2
2004	2
2005	2
2006	6
2007	2
2009	2
2024	0

1

Genetic analysis of von Willebrand's disease in two large pedigrees: a multivariate approach.

Goldin LR, Elston RC, Graham JB, Miller CH. Goldin LR, et al. Am J Med Genet. 1980;6(4):279-93. doi: 10.1002/ajmg.1320060405. Am J Med Genet. 1980. PMID: 6782878

2

Alport syndrome. Molecular genetic aspects.

Hertz JM. Hertz JM. Dan Med Bull. 2009 Aug;56(3):105-52. Dan Med Bull. 2009. PMID: 19728970

3

Autosomal recessive von Willebrand disease type 1 or 2 due to homozygous or compound heterozygous mutations in the von Willebrand factor gene. A single center experience on molecular heterogeneity and laboratory features in 12 families.

Castaman G, Giacomelli S, Rodeghiero F. Castaman G, et al. Acta Haematol. 2009;121(2-3):106-10. doi: 10.1159/000214850. Epub 2009 Jun 8. Acta Haematol. 2009. PMID: 19506356 Review.

4

Forensic STRs as potential disease markers: a study of VWA and von Willebrand's Disease.

Laird R, Schneider PM, Gaudieri S. Laird R, et al. Forensic Sci Int Genet. 2007 Dec;1(3-4):253-61. doi: 10.1016/j.fsigen.2007.06.002. Epub 2007 Jul 13. Forensic Sci Int Genet. 2007. PMID: 19083770

5

MCMC-based linkage analysis for complex traits on general pedigrees: multipoint analysis with a two-locus model and a polygenic component.

Sung YJ, Thompson EA, Wijsman EM. Sung YJ, et al. Genet Epidemiol. 2007 Feb;31(2):103-14. doi: 10.1002/gepi.20194. Genet Epidemiol. 2007. PMID: 17123301

6

Hemorrhagic symptoms and bleeding risk in obligatory carriers of type 3 von Willebrand disease: an international, multicenter study.

Castaman G, Rodeghiero F, Tosetto A, Cappelletti A, Baudo F, Eikenboom JC, Federici AB, Lethagen S, Linari S, Lusher J, Nishino M, Petrini P, Srivastava A, Ungerstedt JS. Castaman G, et al. J Thromb Haemost. 2006 Oct;4(10):2164-9. doi: 10.1111/j.1538-7836.2006.02070.x. J Thromb Haemost. 2006. PMID: 16999850 Free article.

7

Characterization of recessive severe type 1 and 3 von Willebrand Disease (VWD), asymptomatic heterozygous carriers versus bloodgroup O-related von Willebrand factor deficiency, and dominant type 1 VWD.

Michiels JJ, Berneman Z, Gadisseur A, van der Planken M, Schroyens W, van de Velde A, van Vliet H. Michiels JJ, et al. Clin Appl Thromb Hemost. 2006 Jul;12(3):277-95. doi: 10.1177/1076029606291401. Clin Appl Thromb Hemost. 2006. PMID: 16959681 Free article. Review.

8

Von Willebrand's disease: a novel mutation, P1824H and the incidence of R1205H defect among families with dominant quantitative von Willebrand factor deficiency.

Casaña P, Cabrera N, Haya S, Cid AR, Aznar JA. Casaña P, et al. Haematologica. 2006 Aug;91(8):1130-3. Epub 2006 Jul 25. Haematologica. 2006. PMID: 16870550

9

Genetic diagnosis of haemophilia and other inherited bleeding disorders.

Peyvandi F, Jayandharan G, Chandy M, Srivastava A, Nakaya SM, Johnson MJ, Thompson AR, Goodeve A, Garagiola I, Lavoretano S, Menegatti M, Palla R, Spreafico M, Tagliabue L, Asselta R, Duga S, Mannucci PM. Peyvandi F, et al. Haemophilia. 2006 Jul;12 Suppl 3:82-9. doi: 10.1111/j.1365-2516.2006.01263.x. Haemophilia. 2006. PMID: 16684001 Review.

10

Genetic linkage and association analysis in type 1 von Willebrand disease: results from the Canadian type 1 VWD study.

James PD, Paterson AD, Notley C, Cameron C, Hegadorn C, Tinlin S, Brown C, O'Brien L, Leggo J, Lillicrap D; ASSOCIATION OF HEMOPHILIA CLINIC DIRECTORS OF CANADA. James PD, et al. J Thromb Haemost. 2006 Apr;4(4):783-92. doi: 10.1111/j.1538-7836.2006.01860.x. J Thromb Haemost. 2006. PMID: 16634747 Free article.

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